Canonical Allele Identifier: CA2320565957

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709810C= , CM000681.2:g.6709810C=	GRCh38
NC_000019.9:g.6709821C= , CM000681.1:g.6709821C=	GRCh37
NC_000019.8:g.6660821C=	NCBI36
NG_009557.1:g.15842G= , LRG_27:g.15842G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1596G=	ENSP00000512083.1:p.Arg532=
ENST00000695654.1:c.843G=	ENSP00000512085.1:p.Arg281=
ENST00000695655.1:c.660G=	ENSP00000512086.1:n.660G=
ENST00000695692.1:n.1083G=
ENST00000245907.11:c.1719G= MANE Select	ENSP00000245907.4:p.Arg573=
ENST00000245907.10:c.1719G=	ENSP00000245907.4:p.Arg573=
ENST00000600763.1:n.352G=
NM_000064.3:c.1719G=	NP_000055.2:p.Arg573=
NM_000064.4:c.1719G= MANE Select	NP_000055.2:p.Arg573=